9 job matcher din søgning
GE Healthcare, Brøndby
GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry.
Responsible for creating and winning sales opportunities for their products/solutions/services in an assigned territory, and/or in a list of named accounts individually or as part of a One GE Healthcare team.
Act as the clinical/technical expert to establish and continuously develop the relationship with departmental and technical decision makers in their assigned accounts and where applicable work in conjunction with Account Executives and Managers to gain access to C-Suite decision makers.
Indrykket 8. december
The Regulatory Submission Management & Telematics Department is responsible for the critical operational activities in connection with compilation and submission of marketing authorisation applications, regulatory data management and implementation of labelling and manufacturing changes in the production area.
As Regulatory Submission Publisher your main responsibility areas will be:
- Global operational activities related to compilation and publishing of all marketing applications (initial application, variations, renewals, PSUR etc.), including:
- QC and clean-up of documentation for regulatory submissions
- Compilation of regulatory documents
- Provide guidance on standards and technical requirements in relation to publishing etc.
Indrykket 8. december
Chr. Hansen A/S, Hørsholm
Food Culture and Enzymes is the largest Business Unit within Chr. Hansen and work closely with some of the largest global dairy companies providing them with our pioneering product developments.
We are seeking an Indian-speaking top-ten graduate with appreciation of the Indian food and dairy culture to join our Global Application organization in Denmark and France. You must be prepared and committed to continue your career in our application center in India (Mumbai) after around 2-years trainee period in Europe.
- Develop your dairy application skills within the Fresh Dairy, Cheese and BioProtection segments enabling you to provide top-class technical advice and trouble-shooting to our customers
- Plan, perform and report on trials. Hands-on work in the pilot dairy and laboratories will part of your assignments
Indrykket 4. december
Are you fascinated by the intricacies and complexities that make up of a global PV system? Are you motivated by a quality mindset and building quality into processes? If yes, you may be just the person we are looking for to fill this position.
Reporting to the Senior Director, Head of CQA, you will be responsible for execution of the PV audit strategy, including delivery of a risk based audit programme covering the quality and compliance of the PV System. You are also responsible to provide input and advice on processes and areas impacted by Good Pharmacovigilance Practice (GVP) with respect to the requirements of global and local regulations, guidelines and industry best practices. This position has no line management responsibilities, but you will be a vital contributor to our inspiring patient focussed strategy.
Indrykket 4. december
Agilent Technologies Denmark, Glostrup
We are looking for a Process Validation Specialist to lead in the validation and implementation of manufacturing processes and transform broad concepts into structured results-focused projects. You will be responsible for ensuring compliance to the regulatory requirements of the manufacturing processes, facilities, utilities, equipment and analytical instruments qualification processes and activities performed in the Manufacturing facility at Glostrup.
Your key responsibilities will be:
- Responsible for planning, scheduling, and leading validation assignments. Identify gaps related to validation requirements and Global Validation procedures. Drive and close compliance gaps as they are identified.
- Assist/support, as required, in the investigation and closure of non-conformances/events, corrective actions and preventative actions.
Indrykket 1. december
Gubra ApS, Hørsholm
To a vacant position in our growing Peptide Chemistry and Formulation group, Gubra is now looking for a Laboratory technician to join the group. The candidate should have a flair and interest for formulation of peptide drug candidates as well as small molecule test compounds. The candidate is self-motivated and can navigate and collaborate in an energetic organization, and is ready to set ambitious high standards for the output of the group.
Your primary tasks are varied, but include:
- Formulation of peptide and/or small molecule drug candidates for in vivo pharmacology experiments
- Stability determination of peptide drug candidates (chemical and physical stability)
- Biopharmaceutical characterization and analysis of peptides by UPLC
- Data processing and documentation
Indrykket 1. december
Som akademiker vil du indgå i en af funktionens 4 sektioner, hvor du efter gennemført træning vil dele ansvaret for sektionens opgaver med de øvrige akademikere. I arbejdet med vores LEAN aktiviteter vil du tillige kontinuerligt bidrage til skabelsen af den bedste forsyningskæde, hvilket betyder at to dage sjældent er ens.
Du kommer til at indgå i en gruppe der har ansvaret for råvarer og excipients, hvilket indebærer implementering af nye varer i produktionen, råvareafprøvninger, løbende leverandør evalueringer, reklamationer m.m. Du vil også være medansvarlig for at Lundbecks råvarer, excipients, intermediater, API’er og farmaceutiske bulk produkter lever op til myndighedernes GMP krav. Dette indebærer bl a. godkendelse af analyser samt afvigelsesbehandling, udarbejdelse af SOPer, implementering og vedligeholdelse af analyseudstyr.
Indrykket 30. november
Arla Foods, Holstebro, Sweden, UK and Germany
Do you want to pursue a career in Production Management with the potential to be a future leader and role model for the employees at our dairies?
Arla’s Production Management Graduate Programme is a 2-year entry level programme where talented graduates can begin a leadership career at our dairy sites. The programme will take you to 2 different European production sites (Denmark, Sweden, UK and Germany) where you will spend 18 months in your primary location and 6 months abroad.
You will work in conjunction with our Site Directors and middle Managers to work on projects and develop your leadership skills. You will solve complex tasks and bring ideas to the management team for consideration and decision-making.
Indrykket 27. november
We are looking for a Senior Research Scientist to join one of our Discovery Chemistry Groups. As an outstanding medicinal chemist with documented results you have the opportunity to become a Senior Research Scientist in Discovery Chemistry (DC) at the Lundbeck Research Centre in Copenhagen Denmark (DK), and join our quest for new medicines to treat Central Nervous System (CNS) diseases.
As a Senior Research Scientist in a Medicinal Chemistry Group you can expect to be involved in all aspects of the Medicinal Chemistry value chain, and to lead the chemistry component of drug discovery projects. You will be working in a strong team environment within Discovery Chemistry and will form strong and effective collaborations with scientists from other disciplines within Research.
Indrykket 13. november